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首页> 外文期刊>Jornal de Pediatria >Treatment adherence and level of control in moderate persistent asthma in children and adolescents treated with fluticasone and salmeterol ☆ , ☆☆
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Treatment adherence and level of control in moderate persistent asthma in children and adolescents treated with fluticasone and salmeterol ☆ , ☆☆

机译:氟替卡松和沙美特罗治疗的儿童和青少年中度持续性哮喘的治疗依从性和控制水平☆,☆☆

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摘要

Objective: There is a scarcity of studies that assessed the association between adherence to combination therapy and asthma control in pediatric patients. The authors investigated the association between adherence to fluticasone propionate/salmeterol xinafoate combination-metered aerosol and the level of asthma control in children. Methods: This was a prospective observational study of 84 patients aged 5–16 years with moderate persistent asthma, who remained uncontrolled despite the use of 1000 μg/day of inhaled nonextrafine-hydrofluoric alkane-beclomethasone dipropionate in the three months prior to study enrollment. Participants were prescribed two daily doses of FP (125 μg)/salmeterol xinafoate (25 μg) combination by metered aerosol/spacer for six months. Adherence rates were assessed using the device's dose counter after the 2nd, 4th, and 6th months of follow up. Asthma control was assessed using a simplified Global Initiative for Asthma 2014 Report classification. Results: Mean adherence rates after the second, fourth, and sixth months were 87.8%, 74.9%, and 62.1% respectively, for controlled asthma, and 71.7%, 56.0%, and 47.6% respectively, for uncontrolled asthma (all p -values ≤ 0.03). The proportion of children achieving asthma control increased to 42.9%, 67.9% and 89.3% after the 2nd, 4th and 6th months of follow-up, respectively ( p ≤ 0.001). Conclusion: Adherence rates between 87.8% in the 2nd month and 62.1% in the 6th month were strong determinants of asthma control.
机译:目的:缺乏评估儿童坚持联合治疗与控制哮喘之间关系的研究。作者研究了丙酸氟替卡松/昔萘酸沙美特罗联合计量气雾剂的依从性与儿童哮喘控制水平之间的关系。方法:这是一项前瞻性观察性研究,对84名5至16岁的中度持续性哮喘患者进行了研究,尽管入选前三个月使用了每日吸入1000μg/天的吸入非超细氢氟烷烃-倍氯米松双丙酸酯,但仍未得到控制。通过计量的气雾剂/隔离剂为参与者开出每日两次剂量的FP(125μg)/沙美特罗西那福酯(25μg)组合,为期六个月。在随访的第二,第四和第六个月后,使用设备的剂量计数器评估粘附率。哮喘控制使用简化的《 2014年全球哮喘倡议报告》分类进行评估。结果:控制性哮喘在第二,第四和第六个月后的平均依从率分别为87.8%,74.9%和62.1%,对于非控制性哮喘分别为71.7%,56.0%和47.6%(所有p值) ≤0.03)。在随访的第2、4和6个月后,实现哮喘控制的儿童比例分别增加到42.9%,67.9%和89.3%(p≤0.001)。结论:2个月的依从率在87.8%至6个月的依从率是62.1%是哮喘控制的重要决定因素。

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